Canonical Allele Identifier: PA658672150
Gene: VPS35 HGNC NCBI

Linked Data

ClinVar Variation Id: 487668
ClinVar RCV Id: RCV000577720 RCV002225671
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060676.2:p.Gly51Ser
CA8037106
NM_018206.6:c.151G>A